Canonical Allele Identifier: CA2082835516

Gene: BRCA2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32379337G= , CM000675.2:g.32379337G=	GRCh38
NC_000013.10:g.32953474G= , CM000675.1:g.32953474G=	GRCh37
NC_000013.9:g.31851474G=	NCBI36
NG_012772.3:g.68858G= , LRG_293:g.68858G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.8775G=	ENSP00000434898.2:p.Gln2925=
ENST00000528762.2:c.*142G=	ENSP00000433168.2:n.*142G=
ENST00000530893.7:c.8406G=	ENSP00000499438.2:p.Gln2802=
ENST00000665585.2:c.*337G=	ENSP00000499570.2:n.*337G=
ENST00000666593.2:c.8775G=	ENSP00000499256.2:p.Gln2925=
ENST00000700202.2:c.8775G=	ENSP00000514856.2:p.Gln2925=
ENST00000700202.1:c.1242G=	ENSP00000514856.1:p.Gln414=
ENST00000700203.1:n.902G=
ENST00000380152.8:c.8775G= MANE Select	ENSP00000369497.3:p.Gln2925=
ENST00000544455.6:c.8775G=	ENSP00000439902.1:p.Gln2925=
ENST00000614259.2:c.8783G=	ENSP00000506251.1:n.8783G=
ENST00000665585.1:c.1653G=
ENST00000680887.1:c.8775G=	ENSP00000505508.1:p.Gln2925=
ENST00000380152.7:c.8775G=	ENSP00000369497.3:p.Gln2925=
ENST00000528762.1:c.337G=	ENSP00000433168.1:n.337G=
ENST00000544455.5:c.8775G=	ENSP00000439902.1:p.Gln2925=
NM_000059.3:c.8775G= , LRG_293t1:c.8775G=	NP_000050.2:p.Gln2925=
XM_011535203.1:c.8775G=	XP_011533505.1:p.Gln2925=
XM_011535204.1:c.8679G=	XP_011533506.1:p.Gln2893=
XM_011535205.1:c.8755-413G=	XP_011533507.1:n.8755-413G=
NM_000059.4:c.8775G= MANE Select	NP_000050.3:p.Gln2925=